Inositol Monophosphatase Domain Containing 1 (IMPAD1) (Middle Region) Peptide
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- Target See all IMPAD1 products
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Sequence
- YVTTMVCVAV NGKPMLGVIH KPFSEYTAWA MVDGGSNVKA RSSYNEKTPR
- Characteristics
- This is a synthetic peptide designed for use in combination with anti- IMPAD1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Synonyms
- IMP 3 Peptide, RGD1306455 Peptide, gPAPP Peptide, impa3 Peptide, 1110001C20Rik Peptide, AA408880 Peptide, AI451589 Peptide, AL022796 Peptide, B230207P20 Peptide, Jaws Peptide, GPAPP Peptide, IMP-3 Peptide, IMPA3 Peptide, IMPase 3 Peptide, zgc:123256 Peptide, inositol monophosphatase domain containing 1 Peptide, inositol monophosphatase domain containing 1 S homeolog Peptide, Impad1 Peptide, impad1.S Peptide, IMPAD1 Peptide, impad1 Peptide
- Background
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This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
Alias Symbols: GPAPP, IMP 3, IMP-3, IMPA3
Protein Size: 359 - Gene ID
- 54928
- NCBI Accession
- NM_017813, NP_060283
- UniProt
- Q9NX62
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